Theory of light amplification in active fishnet metamaterials

We establish a theory that traces light amplification in an active double-fishnet metamaterial back to its microscopic origins. Based on ab initio calculations of the light and plasmon fields we extract energy rates and conversion efficiencies associated with gain and loss channels directly from Poynting's theorem. We find that for the negative refractive index mode both radiative loss and gain outweigh resistive loss by more than a factor of 2, opening a broad window of steady-state amplification (free of instabilities) accessible even when a gain reduction close to the metal is taken into account.     

Surface interactions of molecular C60 and impact on Ni(100) and Co(0001) film growth: A scanning tunneling microscopy study

Here, the interactions of C₆₀ at the surface of pseudomorphic Ni/Cu(100) and Co/Ru(0001) thin films and its effect on film growth and morphology were determined using in-situ scanning tunneling microscopy (STM) and Auger electron spectroscopy (AES). The novel development of C₆₀-metallic based nanosystems, such as C₆₀ molecular junction transistors, hinges on our ability to understand the factors governing structural stability in these nanosystems and the nature of the bond interactions at the C₆₀–metal interface. In this study, C₆₀ deposited onto the Ni(100) film surface is observed to be fairly immobile and uniformly distributed across the Ni surface. On the Co(0001) film surface however, C₆₀ mobility is observed to be severely limited in some regions and highly mobile in others dependent upon Co film surface reconstruction, resulting in a non-uniform distribution of C₆₀ across the Co film surface. Despite the presence of C₆₀ on the Ni surface, there is no obvious influence of the C₆₀ on further Ni film growth. In contrast, during Co film growth, islands only nucleate and grow from step edges or locally around C₆₀ molecules. The strength of the Co–C₆₀ bond interaction appears stronger than the Co–Co bond on Co film terrace. Generally, the Ni and Co films both continue epitaxial film growth in the presence of molecular C₆₀. AES results indicate the C₆₀ molecules maintain their chemical integrity during growth.     

High-efficiency frequency doubling of continuous-wave laser light

We report on the observation of high-efficiency frequency doubling of 1550?nm continuous-wave laser light in a nonlinear cavity containing a periodically poled potassium titanyl phosphate crystal (PPKTP). The fundamental field had a power of 1.10?W and was converted into 1.05?W at 775?nm, yielding a total external conversion efficiency of 95±1%. The latter value is based on the measured depletion of the fundamental field being consistent with the absolute values derived from numerical simulations. According to our model, the conversion efficiency achieved was limited by the nonperfect mode matching into the nonlinear cavity and by the nonperfect impedance matching for the maximum input power available. Our result shows that cavity-assisted frequency conversion based on PPKTP is well suited for low-decoherence frequency conversion of quantum states of light.     

In vitro reconstitution of eukaryotic ion channels using droplet interface bilayers

The ability to routinely study eukaryotic ion channels in a synthetic lipid environment would have a major impact on our understanding of how different lipids influence ion channel function. Here, we describe a straightforward, detergent-free method for the in vitro reconstitution of eukaryotic ion channels and ionotropic receptors into droplet interface bilayers and measure their electrical activity at both the macroscopic and single-channel level. We explore the general applicability of this method by reconstitution of channels from a wide range of sources including recombinant cell lines and native tissues, as well as preparations that are difficult to study by conventional methods including erythrocytes and mitochondria.     

Observations of PDDTT subject to thermal treatment: correlation between performance and order

We show that polybis(thienyl)thienodia-thiazolethiophene (PDDTT), a high-performance semiconducting polymer for photodetectors and field-effect transistors, has strong performance dependence on annealing temperature. An unprecedented increase of 3 orders of magnitude is observed in both transistor and photoconductive properties. XRD and AFM evidence points to increased ordering in PDDTT films with annealing. This correlation highlights the importance that order has in determining performance in PDDTT and has possible implications in the design of polymers.     

A new family of 1D exchange biased heterometal single-molecule magnets: observation of pronounced quantum tunneling steps in the hysteresis loops of quasi-linear {Mn2Ni3} clusters

First members of a new family of heterometallic Mn/Ni complexes [Mn(2)Ni(3)X(2)L(4)(LH)(2)(H(2)O)(2)] (X = Cl: 1; X = Br: 2) with the new ligand 2-{3-(2-hydroxyphenyl)-1H-pyrazol-1-yl}ethanol (H(2)L) have been synthesized, and single crystals obtained from CH(2)Cl(2) solutions have been characterized crystallographically. The molecular structures feature a quasi-linear Mn(III)-Ni(II)-Ni(II)-Ni(II)-Mn(III) core with six-coordinate metal ions, where elongated axes of all the distorted octahedral coordination polyhedra are aligned parallel and are fixed with respect to each other by intramolecular hydrogen bonds. 1 and 2 exhibit quite strong ferromagnetic exchange interactions throughout (J(Mn-Ni) ≈ 40 K (1) or 42 K (2); J(Ni-Ni) ≈ 22 K (1) or 18 K (2)) that lead to an S(tot) = 7 ground state, and a sizable uniaxial magnetoanisotropy with D(mol) values -0.55 K (1) and -0.45 K (2). These values are directly derived also from frequency- and temperature-dependent high-field EPR spectra. Slow relaxation of the magnetization at low temperatures and single-molecule magnet (SMM) behavior are evident from frequency-dependent peaks in the out-of-phase ac susceptibilities and magnetization versus dc field measurements, with significant energy barriers to spin reversal U(eff) = 27 K (1) and 22 K (2). Pronounced quantum tunnelling steps are observed in the hysteresis loops of the temperature- and scan rate-dependent magnetization data, but with the first relaxation step shifted above (1) or below (2) the zero crossing of the magnetic field, despite the very similar molecular structures. The different behavior of 1 and 2 is interpreted in terms of antiferromagnetic (1) or ferromagnetic (2) intermolecular interactions, which are discussed in view of the subtle differences of intermolecular contacts within the crystal lattice.     

Anomalous thermal expansion in the square-net compounds RE4TGe8 (RE = Yb, Gd; T = Cr-Ni, Ag)

The family of materials RE(4)TGe(8) (RE = Yb, Gd; T = transition metal) exhibits directional zero thermal expansion (ZTE) via a process that is associated with the linking of planar square nets in the third dimension. The Ge square nets in these compounds exhibit commensurate long-range modulations similar to those observed in charge-density-wave compounds. The ZTE is manifested in the plane of the square nets from 10 to 300 K with negligible volume expansion below ～160 K. The specific atomic arrangement in RE(4)TGe(8) enables a Poisson-like mechanism that allows the structure to contract along one direction as it expands only slightly in the perpendicular direction.     

Intercalation in layered metal-organic frameworks: reversible inclusion of an extended π-system

We report the synthesis of layered [Zn(2)(bdc)(2)(H(2)O)(2)] and [Cu(2)(bdc)(2)(H(2)O)(2)] (bdc = benzdicarboxylate) metal-organic frameworks (MOF) carried out using the liquid-phase epitaxy approach employing self-assembled monolayer (SAM) modified Au-substrates. We obtain Cu and Zn MOF-2 structures, which have not yet been obtained using conventional, solvothermal synthesis methods. The 2D Cu(2+) dimer paddle wheel planes characteristic for the MOF are found to be strictly planar, with the planes oriented perpendicular to the substrate. Intercalation of an organic dye, DXP, leads to a reversible tilting of the planes, demonstrating the huge potential of these surface-anchored MOFs for the intercalation of large, planar molecules.     

Progress with the MPIK/UW-PTMS in Heidelberg

The precise determination of the ³He/³H mass ratio, and hence the tritium ??-decay endpoint energy E ₀, is of relevance for the measurement of the electron anti-neutrino mass performed by the Karlsruhe Tritium Neutrino experiment (KATRIN). By determining this ratio to an uncertainty of 1 part in 10¹¹, systematic errors of E ₀ can be checked in the data analysis of KATRIN. To reach this precision, a Penning Trap Mass Spectrometer was constructed at the University of Washington and has been transferred to the Max Planck Institute for Nuclear Physics in Heidelberg at the end of 2008. Since then it is called MPIK/UW-PTMS. Special design features are the utilization of an external ion source and a double trap configuration. The external Penning ion source efficiently ionizes the helium and tritium gas and can give superior elimination of unwanted ion species compared to the previously utilized in-trap-ionization by electrons from a field-emission point. The design as a double Penning trap allows a faster measurement procedure. This should help to avoid problems resulting from long-term drifts in the experimental conditions. Additionally, the laboratory in Heidelberg was carefully prepared to have very stable environmental conditions. Experimental challenges and the first Heidelberg results with the new spectrometer are presented.     

Measurement of Angstrom to Nanometer Molecular Distances with 19F Nuclear Spins by EPR/ENDOR Spectroscopy

Spectroscopic and biophysical methods for structural determination at atomic resolution are fundamental in studies of biological function. Here we introduce an approach to measure molecular distances in bio‐macromolecules using ¹⁹F nuclear spins and nitroxide radicals in combination with high‐frequency (94 GHz/3.4 T) electron–nuclear double resonance (ENDOR). The small size and large gyromagnetic ratio of the ¹⁹F label enables to access distances up to about 1.5 nm with an accuracy of 0.1–1 Å. The experiment is not limited by the size of the bio‐macromolecule. Performance is illustrated on synthesized fluorinated model compounds as well as spin‐labelled RNA duplexes. The results demonstrate that our simple but strategic spin‐labelling procedure combined with state‐of‐the‐art spectroscopy accesses a distance range crucial to elucidate active sites of nucleic acids or proteins in the solution state.